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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1956 4
1957 4
1958 2
1959 1
1960 5
1962 2
1963 1
1964 1
1965 1
1967 3
1968 1
1969 2
1970 2
1971 1
1973 1
1974 2
1975 1
1976 2
1977 1
1978 2
1979 4
1980 1
1981 4
1982 5
1983 3
1984 11
1985 7
1986 4
1987 12
1988 5
1989 6
1990 6
1991 5
1992 14
1993 4
1994 5
1995 15
1996 12
1997 9
1998 7
1999 6
2000 17
2001 11
2002 5
2003 9
2004 15
2005 22
2006 11
2007 15
2008 14
2009 14
2010 20
2011 11
2012 20
2013 18
2014 24
2015 22
2016 24
2017 19
2018 25
2019 17
2020 22
2021 16
2022 16
2023 9
2024 3

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534 results

Results by year

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Page 1
Thalassaemia.
Taher AT, Weatherall DJ, Cappellini MD. Taher AT, et al. Lancet. 2018 Jan 13;391(10116):155-167. doi: 10.1016/S0140-6736(17)31822-6. Epub 2017 Jul 31. Lancet. 2018. PMID: 28774421 Review.
Inherited haemoglobin disorders, including thalassaemia and sickle-cell disease, are the most common monogenic diseases worldwide. Several clinical forms of alpha-thalassaemia and beta-thalassaemia, including the co-inheritance of beta-thalassaemia with haemoglob
Inherited haemoglobin disorders, including thalassaemia and sickle-cell disease, are the most common monogenic diseases worldw …
Hemoglobin E disease and glycosylated hemoglobin.
Yedla N, Kuchay MS, Mithal A. Yedla N, et al. Indian J Endocrinol Metab. 2015 Sep-Oct;19(5):683-5. doi: 10.4103/2230-8210.163211. Indian J Endocrinol Metab. 2015. PMID: 26425484 Free PMC article.
Hemoglobin e syndromes.
Vichinsky E. Vichinsky E. Hematology Am Soc Hematol Educ Program. 2007:79-83. doi: 10.1182/asheducation-2007.1.79. Hematology Am Soc Hematol Educ Program. 2007. PMID: 18024613 Review.
The combination of Hb E and Hb S (Hb SE) results in a sickle cell disease syndrome similar to sickle beta(+) thalassemia. It is important to distinguish Hb E disorders diagnostically because of this marked difference in clinical course among different genotypes. ...Morbidi …
The combination of Hb E and Hb S (Hb SE) results in a sickle cell disease syndrome similar to sickle beta(+) thalassemia. It is impor …
Impacts of beta-thalassemia/hemoglobin E disease on pregnancy outcomes.
Anuruksuwan P, Sirilert S, Luewan S, Tongsong T. Anuruksuwan P, et al. Int J Gynaecol Obstet. 2024 Jan 17. doi: 10.1002/ijgo.15360. Online ahead of print. Int J Gynaecol Obstet. 2024. PMID: 38234105
OBJECTIVE: To compare obstetric outcomes between women with beta-thalassemia/hemoglobin E (beta-thal/HbE) disease and those of low-risk pregnancies, and also between the two subgroups, beta-thal(0) /HbE and beta-thal(+) /HbE disease. ...Pregnancy may b …
OBJECTIVE: To compare obstetric outcomes between women with beta-thalassemia/hemoglobin E (beta-thal/HbE) disease and t …
Hemoglobinopathies: clinical manifestations, diagnosis, and treatment.
Kohne E. Kohne E. Dtsch Arztebl Int. 2011 Aug;108(31-32):532-40. doi: 10.3238/arztebl.2011.0532. Epub 2011 Aug 8. Dtsch Arztebl Int. 2011. PMID: 21886666 Free PMC article.
BACKGROUND: Hemoglobinopathies are among the most common inherited diseases around the world. They have become much more common recently in northern and central Europe, including Germany, due to immigration. ...The highly variable clinical manifestations of the hemoglobino …
BACKGROUND: Hemoglobinopathies are among the most common inherited diseases around the world. They have become much more common recen …
Hydroxyurea for hemoglobin E/beta-thalassemia: a systematic review and meta-analysis.
Algiraigri AH, Kassam A. Algiraigri AH, et al. Int J Hematol. 2017 Dec;106(6):748-756. doi: 10.1007/s12185-017-2307-0. Epub 2017 Aug 7. Int J Hematol. 2017. PMID: 28786080 Review.
Hemoglobin E-beta thalassemia (Hb E/beta-thalassemia) is a distinct, yet common, type of beta-thalassemia, in which the patient co-inherits a beta-thalassemia allele from one parent, and a structural variant, Hb E, from the other parent. ...Hydroxyurea (HU), an oral
Hemoglobin E-beta thalassemia (Hb E/beta-thalassemia) is a distinct, yet common, type of beta-thalassemia, in which the patien
Non-transfusion-dependent thalassemias.
Musallam KM, Rivella S, Vichinsky E, Rachmilewitz EA. Musallam KM, et al. Haematologica. 2013 Jun;98(6):833-44. doi: 10.3324/haematol.2012.066845. Haematologica. 2013. PMID: 23729725 Free PMC article. Review.
The most commonly investigated forms are beta-thalassemia intermedia, hemoglobin E/beta-thalassemia, and alpha-thalassemia intermedia (hemoglobin H disease). ...Ineffective erythropoiesis and peripheral hemolysis, the hallmarks of disease process, lead …
The most commonly investigated forms are beta-thalassemia intermedia, hemoglobin E/beta-thalassemia, and alpha-thalassemia int …
Hemoglobin E-thalassemia disease.
CHATTERJEA JB, SAHA AK, RAY RN, GHOSH SK. CHATTERJEA JB, et al. Indian J Med Sci. 1957 Aug;11(8):553-64. Indian J Med Sci. 1957. PMID: 13474769 No abstract available.
Hemoglobin E-thalassemia disease.
KOCHHAR BR, KATHPALIA PM. KOCHHAR BR, et al. Indian J Med Sci. 1963 Feb;17:138-42. Indian J Med Sci. 1963. PMID: 14034045 No abstract available.
534 results